A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763912



Internal ID19310339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:40915718..40938771hg38UCSC Ensembl
chr9:68988899..69012000hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3823054
hg1923102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078079
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763912
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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